Canonical Allele Identifier: CA190627569
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs971615637
gnomAD v2: 9-21140501-C-G
gnomAD v3: 9-21140502-C-G
gnomAD v4: 9-21140502-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140502C>G , CM000671.2:g.21140502C>G GRCh38
NC_000009.11:g.21140501C>G , CM000671.1:g.21140501C>G GRCh37
NC_000009.10:g.21130501C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*481G>C ENSP00000369578.2:n.*481G>C